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Anti-C12ORF49 Polyclonal Antibody

Catalog No. TMAB-03297 Copy Product Info
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Anti-C12ORF49 Polyclonal Antibody is a Rabbit antibody targeting C12ORF49. Anti-C12ORF49 Polyclonal Antibody can be used in WB.

Anti-C12ORF49 Polyclonal Antibody

Copy Product Info
🥰Excellent
Catalog No. TMAB-03297

Anti-C12ORF49 Polyclonal Antibody is a Rabbit antibody targeting C12ORF49. Anti-C12ORF49 Polyclonal Antibody can be used in WB.

Anti-C12ORF49 Polyclonal Antibody
Pack SizePriceUSA StockGlobal StockQuantity
50 μL$2217-10 days7-10 days
100 μL$3727-10 days7-10 days
200 μL$5277-10 days7-10 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Anti-C12ORF49 Polyclonal Antibody is a Rabbit antibody targeting C12ORF49. Anti-C12ORF49 Polyclonal Antibody can be used in WB.
Ig Type
IgG
Reactivity
Human (predicted:Mouse,Rat,Chicken,Dog,Pig,Cow,Horse,Zebrafish)
Verified Activity
Sample:
U2OS Cell (Human) Lysate at 30 μg
Primary: Anti-C12ORF49 (TMAB-03297) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 24 kD
Observed band size: 35 kD
Application
Recommended Dose
WB: 1:500-2000
Antibody Type
Polyclonal
Host SpeciesRabbit
Subcellular LocalizationSecreted (Potential).
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundEncoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf49 gene product has been provisionally designated C12orf49 pending further characterization.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human C12ORF49
Antigen Species
Human
Gene Name
SPRING1
Gene ID
Protein Name
SREBP regulating gene protein
Uniprot ID
Chemical Properties
Molecular WeightTheoretical: 24 kDa.
Stability & Storage
Stability & StorageStore at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

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